Standard
ISO 14971:2007
[Superseded]ISO 14971:2007 specifies a process for a manufacturer to identify the hazards associated with medical devices, including in vitro diagnostic (IVD) medical devices, to estimate and evaluate the associated risks, to control these risks, and to monitor the effectiveness of the controls.
The requirements of ISO 14971:2007 are applicable to all stages of the life-cycle of a medical device.
Published: 01/03/2007
Pages: 82
Content history
Content history
[Current]
[Superseded]
[Superseded]
[Superseded]
One-time Purchase
Access via web browser on any device
One-time purchase
Single publication
Offline access via PDF^
$122.50 AUD
Inclusive of GSTFormat *
Web Reader (PDF)
Licenses *
1 License (for yourself - not shareable)
Total$122.50 AUD
IMPORTANT